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The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9q.
Published in:
Clinical Genetics, 1994, v. 45, n. 2, p. 88, doi. 10.1111/j.1399-0004.1994.tb04000.x
By:
- Wahlström, J.;
- Ozelius, L;
- Kramer, P.;
- Kyllerman, M.;
- Schuback, D.;
- Forsgren, L.;
- Holmgren, G.;
- Drugge, U.;
- Sanner, G.;
- Fahn, S.;
- Breakefield, X. O.
Publication type:
Article
Cortical sensorimotor alterations classify clinical phenotype and putative genotype of spasmodic dysphonia.
Published in:
European Journal of Neurology, 2016, v. 23, n. 10, p. 1517, doi. 10.1111/ene.13067
By:
- Battistella, G.;
- Fuertinger, S.;
- Fleysher, L.;
- Ozelius, L. J.;
- Simonyan, K.
Publication type:
Article
Haplotype analysis at the DYT1 Locus in ashkenazi jewish patients with occupational hand dystonia.
Published in:
Movement Disorders, 1996, v. 11, n. 2, p. 163, doi. 10.1002/mds.870110208
By:
- Gasser, T.;
- Bove, C. M.;
- Ozelius, L. J.;
- Hallett, M.;
- Charness, M. E.;
- Hochberg, F. H.;
- Breakefield, X. O.
Publication type:
Article
Principles of molecular genetics/Dystonia.
Published in:
Movement Disorders, 1992, v. 7, n. S1, p. 2, doi. 10.1002/mds.870070503
By:
- Breakfield, X. O.;
- Ozelius, L.;
- Kramer, P.;
- De Leon, D.;
- Bressman, S.;
- Risch, N.;
- Schuback, D.;
- Brin, M.;
- Kwiatkowski, D.;
- Hewett, J.;
- Gasser, T.;
- Gusella, J. F.;
- Fahn, S.
Publication type:
Article
Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma.
Published in:
Nature, 1988, v. 332, n. 6161, p. 268, doi. 10.1038/332268a0
By:
- Seizinger, B. R.;
- Rouleau, G. A.;
- Ozelius, L. J.;
- Lane, A. H.;
- Farmer, G. E.;
- Lamiell, J. M.;
- Haines, J.;
- Yuen, J. W. M.;
- Collins, D.;
- Majoor-Krakauer, D.;
- Bonner, T.;
- Mathew, C.;
- Rubenstein, A.;
- Halperin, J.;
- McConkie-Rosell, A.;
- Green, J. S.;
- Trofatter, J. A.;
- Ponder, B. A.;
- Eierman, L.;
- Bowmer, M. I.
Publication type:
Article
Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene.
Published in:
2001
By:
- Hilker, Ruediger;
- Klein, Christine;
- Ghaemi, Mehran;
- Kis, Bernhard;
- Strotmann, Tim;
- Ozelius, Laurie J.;
- Lenz, Olaf;
- Vieregge, Peter;
- Herholz, Karl;
- Heiss, Wolf-Dieter;
- Pramstaller, Peter P.;
- Hilker, R;
- Klein, C;
- Ghaemi, M;
- Kis, B;
- Strotmann, T;
- Ozelius, L J;
- Lenz, O;
- Vieregge, P;
- Herholz, K
Publication type:
journal article
Association studies of Parkinson's disease and parkin polymorphisms.
Published in:
2000
By:
- Klein, Christine;
- Schumacher, Kirsten;
- Jacobs, Helfried;
- Hagenah, Johann;
- Kis, Bernhard;
- Garrels, Jennifer;
- Schwinger, Eberhard;
- Ozelius, Laurie;
- Pramstaller, Peter;
- Vieregge, Peter;
- Kramer, Patricia L.;
- Klein, C;
- Schumacher, K;
- Jacobs, H;
- Hagenah, J;
- Kis, B;
- Garrels, J;
- Schwinger, E;
- Ozelius, L;
- Pramstaller, P
Publication type:
Letter
Genetic linkage studies in autosomal dominant parkinsonism: Evaluation of seven candidate genes.
Published in:
Annals of Neurology, 1994, v. 36, n. 3, p. 387, doi. 10.1002/ana.410360310
By:
- Gasser, T.;
- Wszolek, Z. K.;
- Trofatter, J.;
- Ozelius, L.;
- Uitti, R. J.;
- Lee, C. S.;
- Gusella, J.;
- Pfeiffer, R. F.;
- Calne, D. B.;
- Breakefield, X. O.
Publication type:
Article
Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France?
Published in:
Neurogenetics, 2008, v. 9, n. 2, p. 143, doi. 10.1007/s10048-008-0123-7
By:
- Frédéric, M.;
- Clot, F.;
- Cif, L.;
- Blanchard, A.;
- Dürr, A.;
- Vuillaume, I.;
- Lesca, G.;
- Kreisler, A.;
- Davin, C.;
- Besnard, T.;
- Rousset, F.;
- Thorel, D.;
- Saquet, C.;
- Mechin, D.;
- Ozelius, L.;
- Agid, Y.;
- Barroso, B.;
- Chabrol, B.;
- Chan, V.;
- Clanet, M.
Publication type:
Article
Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi-point linkage analysis.
Published in:
Genetic Epidemiology, 1987, v. 4, n. 5, p. 377, doi. 10.1002/gepi.1370040506
By:
- Kramer, P. L.;
- Ozelius, L.;
- Gusella, J. F.;
- Fahn, S.;
- Kidd, K. K.;
- Breakefield, X. O.;
- Boerecki, I. B.
Publication type:
Article
Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutations.
Published in:
2008
By:
- Raymond D;
- Saunders-Pullman R;
- de Carvalho Aguiar P;
- Schule B;
- Kock N;
- Friedman J;
- Harris J;
- Ford B;
- Frucht S;
- Heiman GA;
- Jennings D;
- Doheny D;
- Brin MF;
- de Leon Brin D;
- Multhaupt-Buell T;
- Lang AE;
- Kurlan R;
- Klein C;
- Ozelius L;
- Bressman S
Publication type:
Journal Article
Dinucleotide repeat polymorphism for the hexabrachion gene (HXB) on chromosome 9q32–34.
Published in:
Human Molecular Genetics, 1992, v. 1, n. 2, p. 141
By:
- Ozelius, L.;
- Schuback, D.E.;
- Stefansson, K.;
- Slaugenhaupt, S.;
- Gusella, J.F.;
- Breakefield, X.O.
Publication type:
Article
The North American Multiple System Atrophy Study Group.
Published in:
Journal of Neural Transmission, 2005, v. 112, n. 12, p. 1687, doi. 10.1007/s00702-005-0381-6
By:
- Gilman, S.;
- May, S. J.;
- Shults, C. W.;
- Tanner, C. M.;
- Kukull, W.;
- Lee, V. M.-Y.;
- Masliah, E.;
- Low, P.;
- Sandroni, P.;
- Trojanowski, J. Q.;
- Ozelius, L.;
- Foroud, T.
Publication type:
Article

Found: 13